MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE
K-Number: K971452 · 1997-05-14
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Device Summary
Frequently Asked Questions
What is the MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE?
MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE is a medical device that received FDA 510(k) clearance on 1997-05-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K971452.
When did MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE receive FDA 510(k) clearance?
MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE received FDA 510(k) clearance on 1997-05-14, under 510(k) number K971452.
Who is the listed applicant for MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE?
The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE?
The FDA product code for MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE is IZZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Siemens Medical Solutions USA, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IZZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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